Purification and interaction analyses of two human lysosomal vitamin B12transporters: LMBD1 and ABCD4

The C-terminal domain of CblD interacts with CblC and influences intracellular cobalamin partitioning

(2013) Carmen Gherasim et al.   BIOCHIMIE

LMBD1 Protein Serves as a Specific Adaptor for Insulin Receptor Internalization

(2013) Linda Tzu-Ling Tseng et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Navigating the B12Road: Assimilation, Delivery, and Disorders of Cobalamin

(2013) Carmen Gherasim et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

An Extended Proteome Map of the Lysosomal Membrane Reveals Novel Potential Transporters

(2013) Agnès Chapel et al.   MOLECULAR & CELLULAR PROTEOMICS

Expression, characterization and ligand specificity of lipocalin-1 interacting membrane receptor (LIMR)

(2013) Renske W. Hesselink et al.   MOLECULAR MEMBRANE BIOLOGY

A Patient With an Inborn Error of Vitamin B12 Metabolism (cblF) Detected by Newborn Screening

(2013) C. M. Armour et al.   PEDIATRICS

Two molybdate/tungstate ABC transporters that interact very differently with their substrate binding proteins

(2013) E. Vigonsky et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Structural features of recombinant MMADHC isoforms and their interactions with MMACHC, proteins of mammalian vitamin B12 metabolism

(2012) Justin C. Deme et al.   MOLECULAR GENETICS AND METABOLISM

Late onset of symptoms in an atypical patient with the cblJ inborn error of vitamin B12 metabolism: Diagnosis and novel mutation revealed by exome sequencing

(2012) Jaeseung C. Kim et al.   MOLECULAR GENETICS AND METABOLISM

Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism

(2012) David Coelho et al.   NATURE GENETICS

Structural Basis of Multifunctionality in a Vitamin B12-processing Enzyme

(2011) Markos Koutmos et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Novel splice site mutations and a large deletion in three patients with the cblF inborn error of vitamin B12 metabolism

(2011) Isabelle R. Miousse et al.   MOLECULAR GENETICS AND METABOLISM

Genetic disorders of vitamin B12 metabolism: eight complementation groups – eight genes

(2010) D. Sean Froese et al.   EXPERT REVIEWS IN MOLECULAR MEDICINE

LMBRD1: the gene for the cblF defect of vitamin B12 metabolism

(2010) Frank Rutsch et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Interaction between MMACHC and MMADHC, two human proteins participating in intracellular vitamin B12 metabolism

(2010) Maria Plesa et al.   MOLECULAR GENETICS AND METABOLISM

A distinct mechanism for the ABC transporter BtuCD–BtuF revealed by the dynamics of complex formation

(2010) Oded Lewinson et al.   NATURE STRUCTURAL & MOLECULAR BIOLOGY

Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism

(2009) Frank Rutsch et al.   NATURE GENETICS

Detergent binding explains anomalous SDS-PAGE migration of membrane proteins

(2009) Arianna Rath et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

70-kDa peroxisomal membrane protein related protein (P70R/ABCD4) localizes to endoplasmic reticulum not peroxisomes, and NH2-terminal hydrophobic property determines the subcellular localization of ABC subfamily D proteins

(2008) Yoshinori Kashiwayama et al.   EXPERIMENTAL CELL RESEARCH

Static light scattering to characterize membrane proteins in detergent solution

(2008) Dirk Jan Slotboom et al.   METHODS